Transferases

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Catalog No.
Product Name
Application
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Product Citation
  1. HLGP Inhibitor

    CP-91149 is a selective glycogen phosphorylase inhibitor.

  2. NMPRTase Inhibitor

    FK866, a highly specific noncompetitive inhibitor of nicotinamide phosphoribosyltransferase, represents a novel mechanism for induction of tumor cell apoptosis.
  3. ACAT/SOAT inhibitor

    YM 750 is reported to act as a SOAT (acyl-CoA:cholesterol acyltransferase, ACAT) inhibitor.
  4. CPT-1 irreversible inhibitor

    Etomoxir is an inhibitor of carnitine palmitoyltransferase A (CPT1), which is required for the oxidation of long-chain acyl CoA esters. Also a strong inhibitor of mitochondrial CPT1 and a candidate as an anti-diabetic drug.
  5. Thymidine phosphorylase activator

    Doxifluridine is a thymidine phosphorylase activator for PC9-DPE2 cells with IC50 of 0.62 μM.
  6. GSTP1-1 inhibitor

    Ezatiostat is a liposomal small-molecule glutathione analog inhibitor of glutathione S-transferase (GST) P1-1 with hematopoiesis-stimulating activity.
  7. Thymidine phosphorylase inhibitor

    Tipiralacil, also known as TPI, is a thymidine phosphorylase inhibitor (TPI).
  8. SphK1 Inhibitor

    PF-543 Citrate is a novel cell-permeant inhibitor of SphK1 with a K(i) of 3.6 nM, PF-543 is sphingosine-competitive and is more than 100-fold selective for SphK1 over the SphK2 isoform.
  9. SphK Inhibitor

    SKI-II is a selective non-lipid inhibitor of sphingosine kinase (IC50 = 0.5 uM).
  10. SphK2 inhibitor

    K145 is a selective SphK2 inhibitor with an IC50 of 4.30?? 0.06 μM , while no inhibition of SphK1 at concentrations up to 10 uM.
  11. SphK2 inhibitor

    K145 is a selective sphingosine kinase-2 (SphK2) inhibitor and anticancer agent.
  12. ATP competitive SK inhibitor

    MP-A08 is a highly selective ATP competitive SK inhibitor that targets both SK1 and SK2 with Kivalues of 6.9 ±  0.8 uM and 27± 3 uM, respectively.

  13. ACAT/SOAT inhibitor

    VULM 1457 is an Acyl-CoA: cholesterol acyltransferase (ACAT) or SOAT inhibitor. VULM 1457 decreases cholesterol levels in the liver and plasma.
  14. ACAT/SOAT inhibitor

    CI 976 is a trimethoxy fatty acid anilide inhibitor of liver and intestinal acyl coenzyme A cholesterol acyltransferase (ACAT) and sterol O-acyltransferase (SOAT). Cl 976 lowers non-high density lipoprotein (non-HDL) cholesterol and increases HDL-cholesterol concentrations.
  15. ACAT inhibitor

    Cyclandelate is an effective inhibitor of rat hepatic acycloenzyme A: cholesterol acyltransferase (ACAT) with IC50 of 80 μM.
  16. PKC activator

    Phorbol 12,13-dibutyrate (Phorbol dibutyrate) is a PKC activator and a potent skin tumor promoter.
  17. RP-64477 is a potent inhibitor of the cholesterol esterifying enzyme Acyl-coenzyme A:cholesterol O-acyltransferase (ACAT).
  18. glutathione analog inhibitor

    Ezatiostat hydrochloride (TER199;TLK199 hydrochloride) is a glutathione analog inhibitor of glutathione S-transferase P1-1 (GSTP1-1).
  19. SphK1 inhibitor

    SKI-178 is a sphingosine kinase 1 (SphK1) inhibitor (IC50 = 0.1-1.8 μM). Induces CDK1-dependent apoptosis in human acute myeloid leukemia cell lines. Active in vivo.

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